Dihydrocytochalasin B - ≥98%(HPLC) , CAS No.39156-67-7

CAS: 39156-67-7 Cat. No.: D139525 Formula: C₂₉H₃₉NO₅ Peso molecolare: 481.62 Numero EC: 254-324-4

GRADE & PURITY ≥98%(HPLC)

Synonyms

MFCD12910542 | EINECS 254-324-4 | 21,22-Dihydrocytochalasan B | 7(S),20(R)-Dihydroxy-16(R)-methyl-10-phenyl-24-oxa(14)cytochalasa-6(12),13(E)-diene-1,23-dione | Cytochalasin H2B | dihydrocytochalasin B | 21,22-Dihydrophomin | 24-OXA(14)CYTOCHALASA-6(12),1

Storage

Store at -20°C

Shipped In

Ice chest + Ice pads

Panoramica

Dihydrocytochalasin B induces changes in cell morphology and motility with no effect on sugar transport. Dihydrocytochalasin B is used as specific marker in studies of high affinity cytochalasin binding sites unrelated to sugar transport. Dihydrocytochalasin B also disrupts the equilibrium between monomeric and polymeric actin.
Marker for high affinity cytochalasin B binding sites. Cytochalasins are used as tools in cytological research, and in in the field of actin polymerisation

Specifications

Sinonimi

MFCD12910542 | EINECS 254-324-4 | 21,22-Dihydrocytochalasan B | 7(S),20(R)-Dihydroxy-16(R)-methyl-10-phenyl-24-oxa(14)cytochalasa-6(12),13(E)-diene-1,23-dione | Cytochalasin H2B | dihydrocytochalasin B | 21,22-Dihydrophomin | 24-OXA(14)CYTOCHALASA-6(12),1

Specifiche e purezza

≥98%(HPLC)

Meccanismi biochimici e fisiologici

Effect on cell motility and morphology similar to that of cytochalasin B; does not inhibit glucose transport.Cytokinesis inhibitor and induces changes in cell morphology and motility. Disrupts actin structure and inhibits ability of serum growth factors t

Condizioni di conservazione di stoccaggio

Store at -20°C

Spedito in

Ice chest + Ice pads

Questo prodotto richiede spedizione a catena fredda. I servizi di terra e altri servizi economici non sono disponibili.

Nota

Wherever possible, you should prepare and use solutions on the same day. However, if you need to make up stock solutions in advance, we recommend that you store the solution as aliquots in tightly sealed vials at -20°C. Generally, these will be useable for up to one month. Before use, and prior to opening the vial we recommend that you allow your product to equilibrate to room temperature for at least 1 hour. Need more advice on solubility, usage and handling? Please visit our frequently asked questions (FAQ) page for more details.

Purezza

≥98%(HPLC)

Nomi e identificatori

• Pubchem Sid: 528769631
• Sorrisi canonici: CC1CCCC(CCC(=O)OC23C(C=CC1)C(C(=C)C(C2C(NC3=O)CC4=CC=CC=C4)C)O)O
• IUPAC Name: (1S,6R,10R,12E,14S,15S,17S,18S,19S)-19-benzyl-6,15-dihydroxy-10,17-dimethyl-16-methylidene-2-oxa-20-azatricyclo[12.7.0.01,18]henicos-12-ene-3,21-dione
• InChIKey: WIULKAASLBZREV-RXPQEOCGSA-N
• INCHI: 1S/C29H39NO5/c1-18-9-7-13-22(31)15-16-25(32)35-29-23(14-8-10-18)27(33)20(3)19(2)26(29)24(30-28(29)34)17-21-11-5-4-6-12-21/h4-6,8,11-12,14,18-19,22-24,26-27,31,33H,3,7,9-10,13,15-17H2,1-2H3,(H,30,34)/b14-8+/t18-,19-,22-,23+,24+,26+,27-,29-/m1/s1
• Isomeri SMILES: C[C@@H]1CCC[C@H](CCC(=O)O[C@]23[C@@H](/C=C/C1)[C@@H](C(=C)[C@H]([C@H]2[C@@H](NC3=O)CC4=CC=CC=C4)C)O)O
• WGK Germania: 3
• Peso molecolare: 481.62
• Reaxy-Rn: 37623011
• Reaxys-RN_link_address: https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=37623011&ln=

Taxonomic Classification

Taxonomy Tree

• Kingdom Organic compounds
  • Superclass Alkaloids and derivatives
    • Classe Cytochalasans
      • Subclass Cytochalasins

• Kingdom: Organic compounds
• Superclass: Alkaloids and derivatives
• Classe: Cytochalasans
• Subclass: Cytochalasins
• Intermediate Tree Nodes: Not available
• Direct Parent: Cytochalasins
• Alternative Parents: Isoindolones Isoindoles Benzene and substituted derivatives Pyrrolidine-2-ones Secondary carboxylic acid amides Carboxylic acid esters Cyclic alcohols and derivatives Secondary alcohols Lactams Lactones Oxacyclic compounds Azacyclic compounds Monocarboxylic acids and derivatives Carbonyl compounds Hydrocarbon derivatives Organic oxides Organonitrogen compounds Organopnictogen compounds
• Molecular Framework: Aromatic heteropolycyclic compounds
• Substituents: Lactone cytochalasin skeleton - Cytochalasin - Isoindolone - Isoindoline - Isoindole - Isoindole or derivatives - Monocyclic benzene moiety - Pyrrolidone - 2-pyrrolidone - Benzenoid - Pyrrolidine - Cyclic alcohol - Secondary alcohol - Secondary carboxylic acid amide - Carboxamide group - Carboxylic acid ester - Lactam - Lactone - Azacycle - Organoheterocyclic compound - Carboxylic acid derivative - Oxacycle - Monocarboxylic acid or derivatives - Organic oxygen compound - Organic nitrogen compound - Organonitrogen compound - Organooxygen compound - Carbonyl group - Organopnictogen compound - Organic oxide - Hydrocarbon derivative - Alcohol - Aromatic heteropolycyclic compound
• Descrizione: This compound belongs to the class of organic compounds known as cytochalasins. These are cytochalasans in which the hydrogenated isoindolone bears a benzyl group.
• External Descriptors: Not available

Data sources

1. Djoumbou Feunang Y, Eisner R, Knox C, Chepelev L, Hastings J, Owen G, Fahy E, Steinbeck C, Subramanian S, Bolton E, Greiner R, and Wishart DS. ClassyFire: Automated Chemical Classification With A Comprehensive, Computable Taxonomy. Journal of Cheminformatics, 2016, 8:61.

DOI: 10.1186/s13321-016-0174-y

Meccanismi d'azione

Proprietà chimiche e fisiche

• Solubilità: Acetone, DMSO, 100% Ethanol, Methanol
• Sensibilità: Light Sensitive
• Punto di fusione (°C): 204°C
• Peso molecolare: 481.600 g/mol
• XLogP3: 3.400
• Hydrogen Bond Donor Count: 3
• Hydrogen Bond Acceptor Count: 5
• Rotatable Bond Count: 2
• Exact Mass: 481.283 Da
• Monoisotopic Mass: 481.283 Da
• Topological Polar Surface Area: 95.900 Ų
• Heavy Atom Count: 35
• Formal Charge: 0
• Complexity: 818.000
• Isotope Atom Count: 0
• Defined Atom Stereocenter Count: 8
• Undefined Atom Stereocenter Count: 0
• Defined Bond Stereocenter Count: 1
• Undefined Bond Stereocenter Count: 0
• The total count of all stereochemical bonds: 1
• Covalently-Bonded Unit Count: 1